![{[Name]}](https://resource.bocsci.com/structure/189264-25-3.gif?v=2025011501)
![{[Name]}](https://resource.bocsci.com/structure/910823-84-6.gif?v=2025011501)
![{[Name]}](https://resource.bocsci.com/structure/1870842-52-6.gif?v=2025011501)
![{[Name]}](https://resource.bocsci.com/structure/131083-16-4.gif?v=2025011501)
![{[Name]}](https://resource.bocsci.com/structure/949108-72-9.gif?v=2025011501)
![{[Name]}](https://resource.bocsci.com/structure/1394861-86-9.gif?v=2025011501)
Inquiry Basket
8-(4-Anilino) Bodipy | CAS 321895-93-6
| Catalog Number | F01-0065 |
| Category | BODIPY |
| Molecular Formula | C19H20BF2N3 |
| Molecular Weight | 339.197 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
BODIPY dyes are used to generate fluorescent conjugates of proteins, nucleotides, oligonucleotides and dextrans, as well as to prepare fluorescent enzyme substrates, fatty acids, phospholipids, lipopolysaccharides, receptor ligands and polystyrene microspheres.
Chemical Information
Product Specification
Application
Computed Properties
| Synonyms | 4-(2,2-difluoro-4,6,10,12-tetramethyl-3-aza-1-azonia-2-boranuidatricyclo[7.3.0.0^{3,7}]dodeca-1(12),4,6,8,10-pentaen-8-yl)aniline |
| IUPAC Name | 4-(2,2-difluoro-4,6,10,12-tetramethyl-3-aza-1-azonia-2-boranuidatricyclo[7.3.0.03,7]dodeca-1(12),4,6,8,10-pentaen-8-yl)aniline |
| Canonical SMILES | [B-]1(N2C(=CC(=C2C(=C3[N+]1=C(C=C3C)C)C4=CC=C(C=C4)N)C)C)(F)F |
| InChI | InChI=1S/C19H20BF2N3/c1-11-9-13(3)24-18(11)17(15-5-7-16(23)8-6-15)19-12(2)10-14(4)25(19)20(24,21)22/h5-10H,23H2,1-4H3 |
| InChIKey | ZYJKXDGIHNXYKQ-UHFFFAOYSA-N |
| Appearance | Dark Yellow Solid |
| Excitation | 561 |
| Emission | 569 |
| Storage | Store at -20°C |
8-(4-Anilino) Bodipy, a fluorescent dye renowned for its exceptional photophysical properties, finds diverse applications in scientific and technological realms. Here are four key applications:
Bioimaging: Widely utilized in bioimaging, 8-(4-Anilino) Bodipy serves as a fluorescent labeling agent for visualizing biological structures at cellular and subcellular scales. Its robust fluorescence properties make it ideal for applications such as confocal microscopy and flow cytometry. By tagging proteins, lipids, or nucleic acids, researchers can explore the dynamic spatial and temporal behaviors of these molecules within living cells, delving deeper into the intricacies of cellular dynamics.
Chemical Sensing: Utilized as a fluorescent probe, 8-(4-Anilino) Bodipy proves valuable in detecting specific ions, molecules, or environmental conditions. Its fluorescence response can be modulated upon binding with analytes, facilitating the development of sensitive and selective sensors. These sensors play a crucial role in diverse applications, from environmental monitoring to diagnostic assays, contributing to the advancement of analytical capabilities in various fields.
Photodynamic Therapy: Unveiling its potential in photodynamic therapy (PDT) for cancer treatment, 8-(4-Anilino) Bodipy demonstrates the ability to generate reactive oxygen species upon light activation, targeting and eliminating cancer cells. Its exceptional photostability and efficient energy transfer position it as a promising candidate for the development of innovative PDT agents, heralding new possibilities in cancer treatment modalities.
Material Science: Within the realm of material science, 8-(4-Anilino) Bodipy can be integrated into polymers to engineer materials boasting unique optical properties. Its applications span the design of light-harvesting materials and fluorescent tags used in organic solar cells and advanced coatings. The dye’s stable fluorescence not only enhances the durability and performance of these materials but also opens avenues for novel advancements in material design and functionality.
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 1 |
| Exact Mass | 339.1718341 g/mol |
| Monoisotopic Mass | 339.1718341 g/mol |
| Topological Polar Surface Area | 34Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 647 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- BODIPY Dyes: Definition, Structure, Synthesis and Uses
- Cyanine Dyes: Definition, Structure, Types and Uses
- Fluorescein Dyes: Definition, Structure, Synthesis and Uses
- Rhodamine Dyes: Definition, Structure, Uses, Excitation and Emission
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
- DNA Staining: Definition, Procedures, Benefits, Dyes and Uses
- Cell Staining: Definition, Principles, Protocols, Dyes, and Uses
- Ion Imaging: Definition, Principles, Benefits, Dyes, and Uses
- Fluorescent Labeling: Definition, Principles, Types and Applications
Recommended Products
Online Inquiry
